Issue 5, 1970

Absolute configuration of trisporic acids and the stereochemistry of cyclization in β-carotene biosynthesis

Abstract

The absolute stereochemistry of trisporic acid C (1) is 1S, 13R; the 1α-methyl, which is equatorial, is selectively labelled by [2-14C]mevalonate, and corresponding chirality at C-1 in [2-14C]mevalonate-labelled β-carotene is thereby indicated with implications for the stereochemistry of cyclization in β-carotene biosynthesis.

Article information

Article type
Paper

J. Chem. Soc. D, 1970, 255-256

Absolute configuration of trisporic acids and the stereochemistry of cyclization in β-carotene biosynthesis

J. D. Bu'Lock, D. J. Austin, G. Snatzke and L. Hruban, J. Chem. Soc. D, 1970, 255 DOI: 10.1039/C29700000255

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements